A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426900



Internal ID205815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59390832..59390836hg38UCSC Ensembl
chr16:59424736..59424740hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426900
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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